# FDA recall Z-2437-2024

> **B Braun Medical Inc** · Class II · device recall initiated 2024-06-14.

## Product

Brand Name: Perfusor Space  Product Name: Perfusor Space Syringe Pump, Non-Wireless  Model/Catalog Number: 8713032U  Product Description: Perfusor Space Syringe Pump, Non-Wireless, Infusion Pump, 1 each  Component: N/A

## Reason for recall

Perfusor Space Syringe Pump's instructions for use previously identified Monoject syringes as an option for use. However, changes to manufacturing to Cardinal Health Monoject syringes may result in issues with recognition, compatibility, and pump performance, such as overdose, underdose, delay in therapy, delay in occlusion alarms, and delay in feeding. Cardinal Health Monoject syringes are not compatible with the indicated pumps.

## Distribution

Domestic distribution nationwide. International distribution to Canada.

## Key facts

- **Recall number:** Z-2437-2024
- **Recalling firm:** B Braun Medical Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-06-14
- **Report date:** 2024-07-31

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Breinigsville, PA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2437-2024

## Citation

> AI Analytics. FDA recall Z-2437-2024. Retrieved 2026-06-26 from https://api.ai-analytics.org/recall/Z-2437-2024. Source: US FDA. Licensed CC0.

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